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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of neuroscience 1 (1989), S. 0 
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The distributions of neurons displaying immunoreactivity for two calcium binding proteins, parvalbumin and 28Kd calbindin, were studied in the thalamus of M. fascicularis. Colocalization experiments were carried out to determine the extent to which parvalbumin- and calbindin-like immunoreactivity was found in the same cells and the extent to which either was localized in GABAergic interneurons. Anterograde and retrograde tracing experiments involving the fluorescent tracer, fast blue, were also used to determine that cells expressing the calcium binding proteins projected upon the cerebral cortex.In the dorsal thalamus, nuclei are distinguished by different patterns of parvalbumin-like and calbindin-like immunoreactivity. In certain nuclei, for example the lateral dorsal and anterior pulvinar, neurons express immunoreactivity for only one of the calcium binding proteins. In others, neurons in different layers, for example the dorsal lateral geniculate nucleus, or in different compartments, for example the intralaminar nuclei, express immunoreactivity for either parvalbumin or calbindin; in other nuclei, for example the ventral group, neurons are mixed and immunoreactivity for parvalbumin and calbindin is commonly colocalized. In the ventral thalamus and epithalamus, similar patterns are observed.Colocalization of parvalbumin- and GABA-immunoreactivity is found in all cells of the reticular nucleus but only in certain cells in selected nuclei of the dorsal thalamus, namely the dorsal lateral geniculate and magnocellular medial geniculate. No calbindin-positive cells are also GABA-positive.Most parvalbumin and/or calbindin positive cells in the dorsal thalamus project to the cerebral cortex, as indicated by the retrograde tracing studies, and many parvalbumin positive fibres entering the cerebral cortex could also be shown to contain fast blue anterogradely transported from a thalamic injection.Most of the major sensory and motor pathways entering the dorsal thalamus express parvalbumin immunoreactivity. The optic tract also expresses calbindin immunoreactivity but most other calbindin positive fibres entering the thalamus ascend in the midbrain tegmentum.The differential distributions of parvalbumin and calbindin implied by these results suggest that thalamic cells belonging to different functional systems and projecting differentially upon the cerebral cortex can be distinguished by differential expression of these or closely related calcium binding proteins. This may yield clues to their differential responsivity to afferent driving.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 307 (1984), S. 267-269 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Three normal cynomolgus monkeys (Macaca fascicularis) and three cats were used. Three other monkeys were anaesthetized and one eye removed 8 or 10 days before they were re-anaesthetized and perfused with buffered 4% paraformal -dehyde. Alternating frozen sections from both sides of the brains were ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 320 (1986), S. 750-753 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In normal monkeys staining reveals GABA-positive somata in all layers of area 17, but concentrated in layers II, IVA and IVC (Fig. \a,b). This distribution pattern agrees with that reported for neurones in monkey area 17 stained immunocyto-chemically for GAD10. The GABA-positive neurones possess ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 62 (1986), S. 438-442 
    ISSN: 1432-1106
    Keywords: Monkey thalamus ; Cytochrome oxidase ; GABA immunocyto-chemistry ; Somatotopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Histochemical staining for a mitochondrial enzyme, cytochrome oxidase demonstrates elongated, rod-like configurations of probable axon terminals in the trigeminal representation of the monkey somatic sensory thalamus. The stained rods are colocalized with similar aggregations of immunocytochemically stained GABAergic thalamic interneurons. Other data suggest the rods also contain clusters of relay neurons projecting to cortical columns, and they are here demonstrated as somatotopic units by micro-electrode mapping and the distribution of afferent fibers. Similar somatotopic rods can be revealed in the rest of the thalamic body representation by the reduction in cytochrome oxidase staining ensuing from the cutting of selected peripheral nerves.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1106
    Keywords: Cerebral cortex ; GABA neurons ; Parvalbumin ; Calbindin ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Calcium ions play a key role in many aspects of neuronal behavior and certain calcium binding proteins that may influence this behavior are differentially distributed in the central nervous system. In this study it is shown that immunoreactivity for calbindin-28 and for parvalbumin is localized in separate populations of inhibitory GABA interneurons in all areas of the neocortex of Old World monkeys. Virtually all GABA neurosn show immunoreactivity for one or other calcium binding protein but, except for a few cells in layer IV, GABA cells do not show immunoreactivity for both proteins. Among the two cell populations, parvalbumin immunoreactivity characterizes basket neurons while calbindin immunoreactivity characterizes double bouquet neurons. These findings suggest that the two GABA cell types differ in their regulation of calcium homeostasis and may yield clues to their different roles in intracortical circuitry.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1106
    Keywords: GABA ; Dorsal lateral geniculate nucleus ; Visual deprivation ; Monkey
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary GABA and glutamate decarboxylase (GAD) immunoreactivities were examined in dorsal lateral geniculate nuclei (LGN) of normal monkeys (Macaca fascicularis) and in monkeys that had one eye injected with tetrodotoxin (TTX) or one eye removed 5 days to 4 weeks prior to sacrifice. As seen in previous studies (Wong-Riley and Carroll 1984) monocular TTX injections or enucleation quickly reduced cytochrome oxidase (CO) staining in layers 2, 3 and 5 of the ipsilateral LGN and in layers 1,4 and 6 of the contralateral LGN. The reduction in CO staining was apparent at all survival times examined. By contrast, GABA and GAD immunostaining in the LGNs were qualitatively normal up to two weeks following enucleation or after 17 days of TTX injections. Quantitative and stereological analyses confirmed that the numerical density and proportion of GABA and GAD neurons do not change in the LGN following two weeks of denervation or deprivation, even though in the same monkeys a reduction in GABA immunostaining was found in deprived-eye columns of area 17. However, with longer survivals, of 3–4 weeks in duration, the number of GABA and GAD immunostained neurons in the deprived/denervated-eye laminae of the LGN was reduced by one-third. These findings demonstrate that the deprivation-induced reduction in GABA and GAD immunoreactivity is delayed in the LGN, by comparison with the visual cortex, and suggest that the effects in the LGN may be relayed through the cortex or that neurotransmitter levels may be regulated by different mechanisms in the two sites.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neurocytology 12 (1983), S. 299-316 
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Commissurally projecting neurons were identified in the monkey first somatic sensory area (SI) by the retrograde axonal transport of horseradish peroxidase (HRP) injected into the contralateral cortex. Neurons identified in this way have large pyramidal somata primarily in layer IIIB of the SI area. Their basal dendrites lie within the terminal plexus of thalamocortical afferents. Electron microscopy was used to examine the synaptic relations of the labelled commissural cells, in particular to determine whether they receive monosynaptic thalamic connections. To do this, retrogradely labelled commissural cells and Golgi-impregnated large pyramidal neurons from layer IIIB were examined ultrastructurally in material in which thalamocortical terminals were degenerating due to a prior lesion of the thalamus. In a significant number of cases degenerating terminals were found to make synapses on the spines or shafts of labelled dendrites. Injections of HRP into SI or into the white matter adjacent to the corpus callosum labelled callosal axons and terminals in the opposite SI. These axons terminated mainly near the somata of the layer IIIB pyramidal cells. Some of their terminals were found to synapse with dendrites receiving synaptic contacts from thalamocortical axon terminals.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary GABAergic neurons have been identified in monkey sensory-motor cerebral cortex by light microscopic, immunocytochemical localization of the GABA synthesizing enzyme, glutamic acid decarboxylase (GAD). All GAD-positive neurons are non-pyramidal cells. Their somata are present in all layers and are evenly distributed across layers II-VI of the motor cortex (area 4), but are found in greater concentrations in layers II, IV and VI of all areas of first somatic sensory cortex (SI; areas 3a, 3b and 1–2). GAD-positive puncta (putative axon terminals) are present throughout the sensory-motor cortex, and they are found immediately adjacent to the somata, dendrites and presumptive axon initial segments of GAD-negative pyramidal cells. In addition, they are observed in close approximation to the somata of both large and small GAD-positive neurons. In area 4, the density of puncta is highest in the superficial cortical layers (layers I-III) and gradually declines throughout the deeper layers. In SI, the highest densities of puncta are present in layer IV, while moderately high densities are found in layers I-III and VI. In areas 3a and 3b, the puncta in layers IV and VI are particularly numerous and form foci that exhibit greater density than adjacent regions. GAD-positive neurons withlarge somata, 15–33 μ in diameter, are present in layers IIIB-VI of all areas. Such cells have many primary dendrites that radiate in all directions. In addition they have axons that ascend either from the superficial aspect of the somata or from primary dendrites, and that exhibit horizontal collateral branches. These neurons closely resemble the large basket cells (Marin-Padilla, 1969; Jones, 1975), and they may give rise to many of the GAD-positive endings surrounding the somata and proximal dendrites of pyramidal cells in layers III-VI. In addition,small GAD-positive somata are present in all layers, but they are most numerous in layers II and IIIA of all areas and in layer IV of SI. The somata and proximal dendrites of these cells vary from a multipolar shape with small, beaded dendrites, found primarily in layer IV, to bitufted and multipolar shapes with larger, smooth dendrites. The diversity of somal sizes and locations, the variety of dendritic patterns, and the different distributions of GAD-positive puncta, all combine to suggest that several different morphological classes of intrinsic comprise the GABA neurons of monkey cerebral cortex.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Golgi-stained neurons of the monkey first somatic sensory cortex (areas 3b and 1–2) and the adjacent area 5 were examined in thionin-counterstained preparations and their dendritic fields related to the position of the major thalamic afferent plexuses (in layers IV and IIIB in area 3b, in layer IIIB only in the other areas and in a subsidiary plexus at the border of layers V and VI). Many types of pyramidal cells of layers IIIB, V and VI have dendrites that consistently branch within the laminae of the thalamic axon terminations: 1. The largest, most deeply situated layer IIIB pyramidal cells have basal dendrites which descend into layer IV of area 3b but become progressively more horizontally oriented in layer IIIB of areas 1–2 and 5. 2. Some layer V pyramidal cells, particularly medium-to-large cells of layer VA, have apical dendrites which give off many branches and spines in both layer IV and layer IIIB of area 3b but only in layer IIIB of areas 1–2 and 5. 3. Some of the modified pyramidal cells of layer VI give rise to apical dendrites that branch profusely in layer IV of area 3b and in layer IIIB of areas 1–2. Many of the non-pyramidal cell types have somata and dendrites among the thalamic afferent plexus. The small spiny (type 7) cells have their somata confined to layer IV of all areas but have an ascending dendritic tuft which is relatively short in area 3b, often barely reaching the upper border of layer IV, but is considerably longer in areas 1–2 and 5, reaching the layer IIIB/IIIA border. Several classes of small aspiny non-pyramidal cells have their somata in layers IIIB and IV of areas 3b and 1–2 but only in layer IIIB of area 5. Large, multipolar neurons (basket or type 1 cells) with somata in layers IIIB to VI of each area have dendrites that branch extensively either in layers IIIB and IV or at the layer V/VI border. It is concluded that virtually all pyramidal cells in layers IIIB, V and VI have substantial dendritic ramifications among the terminations of thalamic afferents. The dendrites of many pyramidal and non-pyramidal cells change their dendritic branching patterns and in some cases the positions of their somata, in a manner that conforms to the change in position of the thalamic afferent plexus from area to area. These observations suggest a close relationship between thalamic terminations and cell form, and may imply that all cells with dendrites among the thalamic terminations in monkey somatic sensory and parietal cortex receive significant numbers of thalamic synapses.
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  • 10
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Neurons in the monkey somatic sensory and motor cortex were labelled immunocytochemically for the GABA synthesizing enzyme, glutamic acid decarboxylase (GAD), and examined with the electron microscope. The somata and dendrites of many large GAD-positive neurons of layers III–VI receive numerous asymmetric synapses from unlabelled terminals and symmetric synapses from GAD-positive terminals. Comparisons with light and electron microscopic studies of Golgi-impregnated neurons suggest that the large labelled neurons are basket cells. Small GAD-positive neurons generally receive few synapses on their somata and dendrites, and probably conform to several morphological types. GAD-positive axons form symmetric synapses on many neuronal elements including the somata, dendrites and initial segments of pyramidal cells, and the somata and dendrites of non-pyramidal cells. Synapses between GAD-positive terminals and GAD-positive cell bodies and dendrites are common in all layers. Many GAD-positive terminals in layers III–VI arise from myelinated axons. Some of the axons form pericellular terminal nests on pyramidal cell somata and are interpreted as originating from basket cells while other GAD-positive myelinated axons synapse with the somata and dendrites of non-pyramidal cells. These findings suggest either that the sites of basket cell terminations are more heterogeneous than previously believed or that there are other classes of GAD-positive neurons with myelinated axons. Unmyelinated GAD-positive axons synapse with the initial segments of pyramidal cell axons or formen passant synapses with dendritic spines and small dendritic shafts and are interpreted as arising from the population of small GAD-positive neurons which appears to include several morphological types.
    Type of Medium: Electronic Resource
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